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Journal Abstract Search

118 related items for PubMed ID: 1227535

  • 1. Growth deficiency, facial dysmorphogenesis and brachydactyly: a new syndrome.
    Frias JL, Guttery EG, Felman AH.
    Birth Defects Orig Artic Ser; 1975; 11(2):30-3. PubMed ID: 1227535
    [No Abstract] [Full Text] [Related]

  • 2. GOMBO syndrome of growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia: a possible "new" recessively inherited MCA/MR syndrome.
    Verloes A, Delfortrie J, Lambotte C.
    Am J Med Genet; 1989 Jan; 32(1):15-8. PubMed ID: 2705477
    [No Abstract] [Full Text] [Related]

  • 3. Unusual type of brachydactyly associated with short stature and facial anomalies. A new syndrome?
    Richieri-Costa A, Colletto GM, Otto PA.
    Am J Med Genet; 1985 Aug; 21(4):637-42. PubMed ID: 4025394
    [Abstract] [Full Text] [Related]

  • 4. New syndrome: mixed hearing loss, mental deficiency, growth retardation, short clubbed digits, and EEG abnormalities in monozygous female twins.
    Pfeiffer RA.
    Am J Med Genet; 1987 Jul; 27(3):639-44. PubMed ID: 3631135
    [No Abstract] [Full Text] [Related]

  • 5. Report of a case and further delineation of the SHORT syndrome.
    Toriello HV, Wakefield S, Komar K, Higgins JV, Waterman DF.
    Am J Med Genet; 1985 Oct; 22(2):311-4. PubMed ID: 4050863
    [Abstract] [Full Text] [Related]

  • 6. Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome?
    Filippi G.
    Am J Med Genet; 1985 Dec; 22(4):821-4. PubMed ID: 4073130
    [Abstract] [Full Text] [Related]

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  • 8. Autosomal dominant Russell-Silver syndrome.
    Al-Fifi S, Teebi AS, Shevell M.
    Am J Med Genet; 1996 Jan 02; 61(1):96-7. PubMed ID: 8741931
    [No Abstract] [Full Text] [Related]

  • 9. Stratton-Parker syndrome: confirmation of a new entity.
    Gabrielli O, Carloni I, Catassi C, Natalini G, Coppa GV, Giorgi P.
    Am J Med Genet; 1994 Feb 01; 49(3):333-6. PubMed ID: 8209896
    [Abstract] [Full Text] [Related]

  • 10. Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs.
    Chitayat D, Hall JG, Couch RM, Phang MS, Baldwin VJ.
    Am J Med Genet; 1990 Sep 01; 37(1):65-70. PubMed ID: 2240046
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  • 12. Partial trisomy 17p12pter, associated with pre and postnatal growth retardation, dysmorphic facial and digital features, developmental delay, and signs of HMSN1 in early childhood.
    Vogt J, Hill S, Brueton L.
    Eur J Med Genet; 2006 Sep 01; 49(5):439-43. PubMed ID: 16488202
    [No Abstract] [Full Text] [Related]

  • 13. A child with sclerocornea, short limbs, short stature, and distinct facial appearance.
    Thompson EM, Winter RM.
    Am J Med Genet; 1988 Jul 01; 30(3):719-24. PubMed ID: 3055984
    [Abstract] [Full Text] [Related]

  • 14. The Aarskog-Scott syndrome in four brothers.
    Archibald RM, German J.
    Birth Defects Orig Artic Ser; 1975 Jul 01; 11(2):25-9. PubMed ID: 1227529
    [No Abstract] [Full Text] [Related]

  • 15. Larsen syndrome in siblings with consanguineous parents.
    Topley JM, Varady E, Lestringant GG.
    Clin Dysmorphol; 1994 Jul 01; 3(3):263-5. PubMed ID: 7526939
    [Abstract] [Full Text] [Related]

  • 16. Hypertrichosis, pigmentary retinopathy, and facial anomalies: a new syndrome?
    Pivnick EK, Wilroy RS, Martens PR, Teather TC, Hashimoto K.
    Am J Med Genet; 1996 Apr 24; 62(4):386-90. PubMed ID: 8723069
    [Abstract] [Full Text] [Related]

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  • 18. Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.
    Yüksel A, Seven M, Deviren A, Söylemez MA, Hacihanefioğlu S, Ulutin T, Cenani A.
    Genet Couns; 1999 Apr 24; 10(3):265-9. PubMed ID: 10546098
    [Abstract] [Full Text] [Related]

  • 19. Weaver syndrome in two Japanese children.
    Kondo I, Mori Y, Kuwajima K.
    Am J Med Genet; 1991 Nov 01; 41(2):221-4. PubMed ID: 1785638
    [Abstract] [Full Text] [Related]

  • 20. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B, Ulmer H, Müller U.
    Am J Med Genet; 1994 Apr 01; 50(2):173-6. PubMed ID: 8010348
    [Abstract] [Full Text] [Related]

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